Recombinant Human MLYCD cell lysate

• Cat.No.: MLYCD-1119HCL

Specification

• Description: The product of this gene catalyzes the breakdown of malonyl-CoA to acetyl-CoA and carbon dioxide. Malonyl-CoA is an intermediate in fatty acid biosynthesis, and also inhibits the transport of fatty acyl CoAs into mitochondria. Consequently, the encoded protein acts to increase the rate of fatty acid oxidation. It is found in mitochondria, peroxisomes, and the cytoplasm. Mutations in this gene result in malonyl-CoA decarboyxlase deficiency.
• Species: Human
• Size: 100 ul
• Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
• Applications: Western Blot

Gene Information

• Gene Name: MLYCD malonyl-CoA decarboxylase [ Homo sapiens ]
• Official Symbol: MLYCD
• Synonyms: MLYCD; malonyl-CoA decarboxylase; malonyl-CoA decarboxylase, mitochondrial; hMCD; MCD; malonyl coenzyme A decarboxylase; MGC59795
• Gene ID: 23417
• mRNA Refseq: NM_012213
• Protein Refseq: NP_036345
• MIM: 606761
• UniProt ID: O95822
• Chromosome Location: 16q24
• Pathway: Malonate semialdehyde pathway, propanoyl-CoA =>Acetyl-CoA, organism-specific biosystem; Malonate semialdehyde pathway, propanoyl-CoA => Acetyl-CoA, conserved biosystem; Metabolic pathways, organism-specific biosystem; Peroxisome, organism-specific biosystem; Peroxisome, conserved biosystem
• Function: lyase activity; malonyl-CoA decarboxylase activity